118 related articles for article (PubMed ID: 24106670)
1. Validation of a stability-indicating hydrophilic interaction liquid chromatographic method for the quantitative determination of vitamin k3 (menadione sodium bisulfite) in injectable solution formulation.
Ghanem MM; Abu-Lafi SA; Hallak HO
Sci Pharm; 2013; 81(3):733-47. PubMed ID: 24106670
[TBL] [Abstract][Full Text] [Related]
2. Validation of a Stability-Indicating RP-HPLC Method for the Simultaneous Determination of Trimethoprim and Sulfadimethoxine Sodium in Oral Liquid Dosage Form.
Ghanem MM; Abu-Lafi SA
Sci Pharm; 2013; 81(2):459-74. PubMed ID: 23833713
[TBL] [Abstract][Full Text] [Related]
3. Development and validation of a stability-indicating HPLC method for the simultaneous determination of sulfadiazine sodium and trimethoprim in injectable solution formulation.
Ghanem MM; Abu-Lafi SA
Sci Pharm; 2013; 81(1):167-82. PubMed ID: 23641336
[TBL] [Abstract][Full Text] [Related]
4. Development of a Stability-Indicating RP-UPLC Method for Rapid Determination of Metaxalone and its Degradation Products in Solid Oral Dosage Form.
Trivedi RK; Patel MC
Sci Pharm; 2012; 80(2):353-66. PubMed ID: 22896822
[TBL] [Abstract][Full Text] [Related]
5. A Stability Indicating Method for the Determination of the Antioxidant Sodium Bisulfite in Pharmaceutical Formulation by RP-HPLC Technique.
Trivedi HK; Patel MC
Sci Pharm; 2011; 79(4):909-20. PubMed ID: 22145114
[TBL] [Abstract][Full Text] [Related]
6. Development and Validation of a Stability-Indicating RP-HPLC Method for the Determination of Process-Related Impurities and Degradation Products of Rabeprazole Sodium in Pharmaceutical Formulation.
Kumar N; Sangeetha D
Sci Pharm; 2013; 81(3):697-711. PubMed ID: 24106668
[TBL] [Abstract][Full Text] [Related]
7. Development of a Stability-Indicating RP-HPLC Method for the Determination of Rupatadine and its Degradation Products in Solid Oral Dosage Form.
Trivedi HK; Patel MC
Sci Pharm; 2012; 80(4):889-902. PubMed ID: 23264938
[TBL] [Abstract][Full Text] [Related]
8. Stability-Indicating LC Method for the Determination of Prasugrel Hydrochloride in Pharmaceutical Dosage Form.
Ahirrao VK; Patil CS; Bembalkar SB; Ubale SB; Marathe RP; Nawale RB; Landge MG; Pawar RP
Sci Pharm; 2012; 80(2):379-91. PubMed ID: 22896824
[TBL] [Abstract][Full Text] [Related]
9. [Confirmation of unknown additives in enrofloxacin powder].
Xiong Y; Wang C; Liu J; Shi H; Wang Y; Sun Y; Yu J
Se Pu; 2021 Jun; 39(6):633-641. PubMed ID: 34227324
[TBL] [Abstract][Full Text] [Related]
10. A Validated Stability-Indicating RP-UPLC Method for Simultaneous Determination of Desloratadine and Sodium Benzoate in Oral Liquid Pharmaceutical Formulations.
Kumar N; Sangeetha D; Reddy PS; Prakash L
Sci Pharm; 2012; 80(1):153-65. PubMed ID: 22396911
[TBL] [Abstract][Full Text] [Related]
11. Development and Validation of a New Stability-Indicating RP-UPLC Method for the Quantitative Determination of Bromfenac Sodium and Its Impurities in an Ophthalmic Dosage Form.
Koppala S; Reddy VR; Anireddy JS
J Chromatogr Sci; 2016 Oct; 54(9):1514-1521. PubMed ID: 27270417
[TBL] [Abstract][Full Text] [Related]
12. UPLC and LC-MS studies on degradation behavior of irinotecan hydrochloride and development of a validated stability-indicating ultra-performance liquid chromatographic method for determination of irinotecan hydrochloride and its impurities in pharmaceutical dosage forms.
Kumar N; Sangeetha D; Reddy SP
J Chromatogr Sci; 2012 Oct; 50(9):810-9. PubMed ID: 22661461
[TBL] [Abstract][Full Text] [Related]
13. A validated stability-indicating liquid chromatographic method for determination of degradation impurities and diastereomers in voriconazole tablets.
Shaikh KA; Patil AT
Sci Pharm; 2012; 80(4):879-88. PubMed ID: 23264937
[TBL] [Abstract][Full Text] [Related]
14. Development and Validation of a Novel Stability-Indicating RP-HPLC Method for the Simultaneous Determination of Halometasone, Fusidic Acid, Methylparaben, and Propylparaben in Topical Pharmaceutical Formulation.
Goswami N; Gupta VR; Jogia HA
Sci Pharm; 2013; 81(2):505-18. PubMed ID: 23833716
[TBL] [Abstract][Full Text] [Related]
15. A validated stability-indicating liquid chromatographic method for the determination of retapamulin in topical dosage form.
Nalwade S; Reddy VR
J Chromatogr Sci; 2014 Mar; 52(3):238-45. PubMed ID: 23510782
[TBL] [Abstract][Full Text] [Related]
16. Stability indicating LC method for rapid determination of related substances of O-desmethyl venlafaxine in active pharmaceutical ingredients and pharmaceutical formulations.
Rao KV; Reddy KP; Kumar YR
J Chromatogr Sci; 2014; 52(10):1247-54. PubMed ID: 24474426
[TBL] [Abstract][Full Text] [Related]
17. A novel automated hydrophilic interaction liquid chromatography method using diode-array detector/electrospray ionization tandem mass spectrometry for analysis of sodium risedronate and related degradation products in pharmaceuticals.
Bertolini T; Vicentini L; Boschetti S; Andreatta P; Gatti R
J Chromatogr A; 2014 Oct; 1365():131-9. PubMed ID: 25242223
[TBL] [Abstract][Full Text] [Related]
18. Stability-indicating HPLC method for the determination of darunavir ethanolate.
Reddy BV; Jyothi G; Reddy BS; Raman NV; Reddy KS; Rambabu C
J Chromatogr Sci; 2013; 51(5):471-6. PubMed ID: 23097581
[TBL] [Abstract][Full Text] [Related]
19. Stability-Indicating RP-HPLC Method for the Simultaneous Estimation of Doxofylline and Terbutalinesulphate in Pharmaceutical Formulations.
Samanthula G; Yadiki K; Saladi S; Gutala S; Surendranath KV
Sci Pharm; 2013; 81(4):969-82. PubMed ID: 24482767
[TBL] [Abstract][Full Text] [Related]
20. Development and validation of a specific stability indicating high performance liquid chromatographic method for valsartan.
Rao K; Jena N; Rao M
J Young Pharm; 2010 Apr; 2(2):183-9. PubMed ID: 21264123
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
